Home Other Building Blocks 818-72-4
818-72-4,MFCD00004588
Catalog No.:AA003EI9

818-72-4 | 1-Octyn-3-ol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
98%
in stock  
$13.00   $9.00
- +
25g
98%
in stock  
$58.00   $41.00
- +
100g
98%
in stock  
$218.00   $153.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA003EI9
Chemical Name:
1-Octyn-3-ol
CAS Number:
818-72-4
Molecular Formula:
C8H14O
Molecular Weight:
126.1962
MDL Number:
MFCD00004588
SMILES:
CCCCCC(C#C)O
Properties
Properties
 
BP:
169.6 °C at 760 mmHg  
Form:
Liquid  
MP:
-60 °C  
Refractive Index:
n20/D 1.441(lit.)  
Solubility:
3.4g/l  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
98.4  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
4  
Undefined Atom Stereocenter Count:
1  
XLogP3:
2  

Literature

Title: Functional characterization of the octenol receptor neuron on the maxillary palps of the yellow fever mosquito, Aedes aegypti.

Journal: PloS one 20110101

Title: Characterization of an enantioselective odorant receptor in the yellow fever mosquito Aedes aegypti.

Journal: PloS one 20090101

Title: Reverse and conventional chemical ecology approaches for the development of oviposition attractants for Culex mosquitoes.

Journal: PloS one 20080101

Title: Evaluation of the enantiomers of 1-octen-3-ol and 1-octyn-3-ol as attractants for mosquitoes associated with a freshwater swamp in Florida, U.S.A.

Journal: Medical and veterinary entomology 20071201

Title: A straightforward synthesis of (-)-phaseolinic acid.

Journal: The Journal of organic chemistry 20041112

Title: Novel chemoenzymatic strategy for the synthesis of enantiomerically pure secondary alcohols with sterically similar substituents.

Journal: The Journal of organic chemistry 20030627

Title: Practical enantioresolution of alcohols with 2-methoxy-2-(1-naphthyl)propionic acid and determination of their absolute configurations by the (1)H NMR anisotropy method.

Journal: Chirality 20020101

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SDS
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